Iridoids from Scrophularia Genus Javier De Santos Galindez, Lidia Fernández Matellano and Ana M

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Iridoids from Scrophularia Genus Javier De Santos Galindez, Lidia Fernández Matellano and Ana M Iridoids from Scrophularia Genus Javier de Santos Galindez, Lidia Fernández Matellano and Ana M. Díaz Lanza* Laboratorio de Farmacognosia, Departamento de Farmacologfa, Facultad de Farmacia, Universidad de Alcalä, 28871 Alcalä de Henares, Madrid, Espana. Fax: 918854660. E-mail: [email protected] * Author for correspondence and reprint requests Z. Naturforsch. 56c, 513-520 (2001); received February 6/March 12, 2001 Iridoid Gglycosides, Scrophularia, Scrophularia scorodonia We report here an updated summary about iridoid composition of a series from the genus Scrophularia which have been investigated until now from a phytochemistry point of view. In addition a list is included about iridoids isolated in our laboratory from different plant parts of Scrophularia scorodonia L.,which are compared with iridoids from some species of the Scrophularia genus. The present study may serve as a current information to researchers working on phytochemistry and pharmacological aspects from the Scrophularia genus and possibly to serve as a new starting point for future investigations. Iridoid glycosides such as harpagoside, aucubo- Mnatsakanyan, 1989), Scrophularia chrisantha side and harpagide are of particular interest to (Babayan and Mnatsakanyan, 1989), Scrophularia botanists because of their potential value in chem- ningpoensis (Quian et al., 1992; Ming et al., 1999), osystematics to elucidate phylogenetic relation­ Scrophularia leucoclada (Saatov and Abdullaev, ships (Bianco, 1990; Luczak and Swiatek, 1978). 1996), Scrophularia vernalis (Swiatek and Krzac- The Scrophularia genus is represented by more zek, 1976) and Scrophularia koraiensis nakai than 300 species. But only a few species have been (Pachaly et a l, 1994) (Table II). Acylated 6-O-a- investigated from a phytochemical and pharmaco­ L-rhamnopyranosylcatalpol are common in genus logical point of view. We have now examined spe­ Scrophularia: Scrophularia scopolii var. scopolii cies from genus Scrophularia which have been in­ (Calis et al., 1988), Scrophularia nodosa (Weinges vestigated from a phytochemical point of view, and and von der Eltz, 1978), Scrophularia spicata report here the results of the literature search. In (Zhang et a l, 1992), Scrophularia ilwensis (Calis et genus Scrophularia the following iridoid glyco­ a l, 1993), Scrophularia auriculata (Giner et al., sides have been found till now: Aucuboside, 6'- 1991; 1998), Scrophularia koelzii (Bhandari et al., cinnamoylaucuboside (scrophularioside), 10-0-ß- 1992) and Scrophularia koraiensis nakai (Pachaly glucosylaucuboside and scropheanoside I in: Scro­ et al., 1994) (Table III). Catalpol, methylcatalpol, phularia canina (Berdini et al., 1991), Scrophularia ajugol and laterioside were found only in some alata Gilib (Swiatek and Broda, 1967), Scrophula­ species : Scrophularia ningpoensis (Qian et a l, ria grossheimi (Akhmedov, 1970), Scrophularia 1992), Scrophularia vernalis (Swiatek and Krzac- nodosa (Weinges and von der Eltz, 1978), Scro­ zek, 1976), Scrophularia lateriflora (Swiatek et a l, phularia ningpoensis (Qian et al., 1992), Scrophu­ 1981), Scrophularia ilwensis (Calis et a l, 1993). laria lateriflora (Swiatek et al., 1981), Scrophularia The presence of picroside I was detected only in vernalis (Swiatek and Krzacek, 1976), Scrophula­ one species, Scrophularia lateriflora (Swiatek et al ., ria ilwensis (Calis et al., 1993) and Scrophularia 1981) (Tables IV, V). koraiensis nakai (Pachaly et al., 1994) (Table I). In the course of a search for biologically active Ester derivates of harpagide in: Scrophularia substances in S. scorodonia we have isolated sev­ canina (Berdini et al., 1991), Scrophularia spicata eral iridoids from leaves and stems, flowers and (Zhang et al., 1992), Scrophularia ilwensis (Calis et roots from this species. al., 1993), Scrophularia buergeriana (Kitagawa et For leaves and stems we have reported, bartsio- al., 1967), Scrophularia grossheimi (Akhmedov, side, aucuboside, harpagoside, 8-O-ds-cinnamoyl- 1970), Scrophularia nodosa (Weinges and von der harpagide, 8-O-acetyl-harpagide and one new iri­ Eltz, 1978), Scrophularia variegata (Babayan and doid 6-0-a-L-(3"-0-acetyl-2"-0-rram-cinnamoyl)- 0939-5075/2001/0700-0513 $ 06.00 © 2001 Verlag der Zeitschrift für Naturforschung, Tübingen ■ www.znaturforsch.com • D Dieses Werk wurde im Jahr 2013 vom Verlag Zeitschrift für Naturforschung This work has been digitalized and published in 2013 by Verlag Zeitschrift in Zusammenarbeit mit der Max-Planck-Gesellschaft zur Förderung der für Naturforschung in cooperation with the Max Planck Society for the Wissenschaften e.V. digitalisiert und unter folgender Lizenz veröffentlicht: Advancement of Science under a Creative Commons Attribution Creative Commons Namensnennung 4.0 Lizenz. 4.0 International License. 514 J. de Santos Galindez et al. ■ Iridoids from Scrophularia Genus rhamnopyranosylcatalpol (scorodioside) (Fernan­ side, harpagoside and 8-O-acetyl-harpagide. These dez Matellano et al., 1995a; Fernandez Matellano compounds have also been isolated from flowers et al., 1995b). of this species, except aucuboside. Scorodioside, Different catalpol derivates have been isolated the new iridoid glycoside isolated from leaves and in this species: 6-0-a-L-(3"-0-fram' and cis p- stems, has also been identified in flowers. As coumaroyl)-rhamnopyranosylcatalpol and 6-O-a- shown in Table VI there is a different distribution L-(2"-0-rra«5-p-coumaroyl)-rhamnopyranosyl- between all plant parts. catalpol (saccatoside) have been reported in flow­ Identification and assigment of the isolated ers; 6-0-a-L-(2"-0-acetyl-3",4"-0-di-frans-cinna- compounds were performed on the basis of UV moyl)-rhamnopyranosylcatalpol (scropolioside B) spectral data, !H and 13CNMR. and 6-O-methylcatalpol in roots from S. scoro- donia (De Santos et al., 1998). Results and Discussion It is of interest to compare the presence and dis­ We have compiled a first listing of iridoids oc­ tribution of some of these iridoids in different currence in Scrophularia genus (Table VII). From plant parts, because a different composition has the distribution of iridoids listed it can be con­ been found in leaves, stems, flowers and roots (Ta­ cluded that the presence of aucuboside (52.9%), ble VI). We have detected the presence of harpag- harpagide (47.05%), harpagoside (47.05%) and 8- ide for the first time in leaves, stems and roots O-acetylharpagide (41.17%) is not rare in species from S. scorodonia. In roots, we have isolated and of the genus, and we have also isolated these com­ identified different iridoids: bartsioside, aucubo- pounds from Scrophularia scorodonia. Table I. Aucuboside, scrophularioside, bartsioside and 10-0-ß-glucosylaucuboside. Compound R Species R eference Aucuboside R1=R2=R3= H S. nodosa (Weinges and von der Eltz, 1978) R4=OH S. gross heim i (Akhmedov, 1970) S. lateriflora (Swiatek et al., 1981) S. canina (Berdini et al., 1991) S. ningpoensis (Quian et al., 1992) S. il wens is (Calis et al., 1993) S. scorodonia (Fernandez et al., 1995 a) S. alata (Swiatek and Broda, 1967) S. vernalis (Swiatek and Krzaczek, 1976) Scrophularioside R1=R2=H S. lateriflora (Swiatek et al., 1981) R3=C6H sCH=CH-CO R 4=O H 10-0-ß-Glucosylaucuboside R1=R3=H S. canina (Berdini et al., 1991) R2=ß-D-GLUCOSA R4=OH Bartsioside R1=R2=R3=R4=H S. scorodonia (Fernandez et al., 1995 a) Scropheanoside I R1=R2=R3=H S. koraiensis (Pachaly et al., 1994) R4 = 4"-0-(p-0CH,-m-0H-ChHvCH=CH-C0) - ß-D-RHAMNOSA J. de Santos Galindez et al. • Iridoids from Scrophularia Genus 515 Table II. Derivatives of harpagide. Compound R Species Reference Harpagide R1=H S. nodosa (Weinges and von der Eltz, 1978) R2=H S. grossheimi (Akhmedov, 1970) S. variegata (Babayan and Mnatsakanyan, 1989) S. chrisantha (Babayan and Mnatsakanyan, 1989) S. ningpoensis (Quian et al., 1992) S. ilwensis (Calis et al., 1993) S. koraiensis (Pachaly et al., 1994) S. leucoclada (Saatov et al., 1996) S. scorodonia 8-O-Acetyl-harpagide Rl=CH^-CO- S. nodosa (Weinges and von der Eltz, 1978) R2=H S. vernalis (Swiatek and Krzaczek, 1976) S. variegata (Babayan and Mnatsakanyan, 1989) S. chrisantha (Babayan and Mnatsakanyan, 1989) S. canina (Berdini et al., 1991) S. ilwensis (Calis et al., 1993) S. scorodonia (Fernandez et al., 1995 a) S. leucoclada (Saatov et al., 1996) 8-0-(p-Methoxycinnamoyl)- r i =c h , o -c 6h 4c h =c h -c o harpagide R2=H S. buergeriana (Kitagawa et al., 1967) S. variegata (Babayan and Mnatsakanyan, 1989) S. chrisantha (Babayan and Mnatsakanyan, 1989) 8-O-fra/zs-cinnamoylharpagide Rl=C6Hs-CH=CH-CO (harpagoside) R2=H S. buergeriana (Kitagawa et al., 1967) S. vernalis (Swiatek and Krzaczek, 1976) S. variegata (Babayan and Mnatsakanyan, 1989) S. chrisantha (Babayan and Mnatsakanyan,,1989) S. ningpoensis (Quian et al., 1992) S. spicata (Zhang et al., 1992) S. koraiensis (Pachaly et al., 1994) S. scorodonia (Fernandez et al., 1995 a) 8-0-czs-cinnamoyI-harpagide Rl=C6Hs-CH=CH-CO- S. scorodonia (Fernandez et al., 1995 b) R2=H 8-0-ds-feruloyl-harpagide Rl=Feruloyl- S. ningpoensis (M ing et al., 1999) R2=H OH 8-0-(2-hydroxy-cinnamoyl)- Rl=C6H,-CH=C-CO- S. ningpoensis (M ing et al., 1999) harpagide R2=H 6-O-a-d-galactopyranosyl- R1=H S. ningpoensis (Ming et al., 1999) harpagide R2=d-galactopyranosyl On the other hand, iridoids derived from aucu- some of this iridoids have been reported only in boside are rarer in the genus Scrophularia, they one species: koelzioside in S. koelzii, scropolio- appear only in some species, such as scrophulario- sides A and B in S. scopolii and S. auriculata , side in S. lateriflora , lO-O-ß-glucosylaucuboside in scrospioside B in S. spicata , scropheanoside II and S. canina and scropheanoside I in S. koraiertsis 6-0-a-L-(2"-0-acetyl-3",4"-0-di-/?-methoxycinna- (Table I). moyl) rhamnopyranosylcatalpol in S. koraiertsis Moreover it is well known that species of Scro­ and S.auriculata, respectively. Picroside I has been phularia contain catalpol derivates (Table III), but detected only in S. lateriflora and 6-0-(ß-D-xylo- 516 J. de Santos Galindez et al.
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